Validation Engineer - Kentucky

Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec’s mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals.

Valspec’s projects are critical to the industry, and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies.

Senior CQV Engineer (Cleaning Validation & Data Integrity)

Location: Lexington, KY (Onsite) Duration: 6+ Month Contract Travel/Per Diem Available Industry: Pharmaceutical / Animal Health Manufacturing

About the Opportunity

Valspec is seeking a Senior CQV Engineer to support a high-impact Cleaning Validation and Data Integrity initiative at a pharmaceutical manufacturing facility in Lexington, Kentucky.

This consultant will lead validation activities supporting manufacturing suites, process equipment, and laboratory systems within a regulated GMP environment. The project includes development and execution of cleaning validation strategies, remediation planning, SOP creation, data integrity assessments, and cross-functional collaboration with Engineering, Quality, Manufacturing, and Laboratory teams.

The facility manufactures veterinary pharmaceutical products in powder, tablet, and granule dosage forms and operates multiple manufacturing suites as well as quality control laboratory operations utilizing HPLC, stability, incubation, dissolution, and analytical testing equipment.

Responsibilities

Lead Cleaning Validation activities from planning through execution

Develop and execute cleaning validation protocols and reports

Design and support swab recovery studies and cleaning validation methods

Establish worst-case product and equipment groupings using scientific and risk-based approaches

Support protocol execution and field verification activities within manufacturing operations

Author and revise validation documentation including:

Validation Plans

Risk Assessments

Protocols

Summary Reports

SOPs

Remediation Plans

Evaluate existing cleaning procedures and implement improvements where necessary

Perform Data Integrity assessments on laboratory systems and equipment

Identify compliance gaps and develop corrective actions and remediation strategies

Partner with Quality and Regulatory stakeholders to ensure alignment with current GMP expectations

Support investigations, deviations, and change control activities related to validation programs

Provide technical leadership and mentorship to project team members as required

Required Qualifications

Bachelor's Degree in Engineering, Chemistry, Life Sciences, Pharmaceutical Sciences, or related discipline

10+ years of CQV, Validation, or Quality Engineering experience within regulated pharmaceutical, biotech, medical device, or animal health manufacturing environments

Demonstrated Cleaning Validation experience including protocol development and execution

Strong understanding of current GMP regulations and FDA expectations

Experience authoring and reviewing validation lifecycle documentation

Experience executing IQ/OQ/PQ activities for manufacturing and laboratory equipment

Proven ability to work independently and interact directly with client leadership

Excellent technical writing and communication skills

Preferred Qualifications

Oral solid dose manufacturing experience

Experience supporting powder, blending, tableting, filling, packaging, or related pharmaceutical operations

Swab method development and recovery study experience

Data Integrity assessment and remediation experience

Laboratory equipment qualification experience

Familiarity with HPLC, dissolution, stability, incubation, and analytical laboratory systems

Experience supporting FDA inspections and audit readiness initiatives

Previous consulting experience within pharmaceutical manufacturing environments

Ideal Candidate

We are seeking a hands-on consultant who can operate as both a technical subject matter expert and a project leader. The ideal candidate is comfortable working directly with Quality, Manufacturing, Engineering, and Laboratory stakeholders while driving validation deliverables independently.

Candidates with strong CQV backgrounds from biotech facilities are encouraged to apply, particularly those who have supported equipment qualification, validation remediation programs, laboratory systems, and cleaning validation initiatives.

Why This Project?

Long-term onsite engagement in Lexington, KY

Travel and per diem support available

High-visibility project with direct client interaction

Blend of Cleaning Validation and Data Integrity initiatives

Opportunity to lead validation strategy and execution rather than simply execute protocols

Immediate impact within a regulated GMP manufacturing environment

Why Join Valspec?

At Valspec, we offer more than just a job — we provide a career experience rooted in a standout culture, collaborative environment, and a strong sense of ownership. As an Employee Stock Ownership Plan (ESOP) company, every team member has a stake in our success, fostering a shared commitment to excellence and innovation. We also offer a highly competitive benefits package, including:

Premium medical coverage

401(k) with company match

Tuition reimbursement

Unique performance incentives

And more — all designed to support your growth, well-being, and future.

Join a team where your contributions matter, your development is prioritized, and your success is shared.

When receiving e-mails from a Proconex or Valspec recruiter, you will only receive e-mails from addresses ending in @proconexdirect.com, @proconex.net or @valspec.net. Any other domains are impersonations and should be ignored.

Candidates must be legally eligible to work in the United States without company sponsorship. Also, we are not interested in working on a corp-to-corp basis with other companies at this time.

Any third-party unsolicited resume submission(s) will immediately become the property of Valspec. Valspec will not pay any fee to a submitting employment agency, person, or entity unless a signed agreement is established.

Valspec is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to providing a professional environment free of any discrimination or harassment, and we are proud to be a Drug-Free Workplace.